SG11201401032YA - (4-phenylimidazol-2-yl) ethylamine derivatives useful as sodium channel modulators - Google Patents

(4-phenylimidazol-2-yl) ethylamine derivatives useful as sodium channel modulators

Info

Publication number
SG11201401032YA
SG11201401032YA SG11201401032YA SG11201401032YA SG11201401032YA SG 11201401032Y A SG11201401032Y A SG 11201401032YA SG 11201401032Y A SG11201401032Y A SG 11201401032YA SG 11201401032Y A SG11201401032Y A SG 11201401032YA SG 11201401032Y A SG11201401032Y A SG 11201401032YA
Authority
SG
Singapore
Prior art keywords
phenylimidazol
sodium channel
derivatives useful
channel modulators
ethylamine derivatives
Prior art date
Application number
SG11201401032YA
Inventor
Sharanjeet Kaur Bagal
Mark Ian Kemp
Duncan Charles Miller
Yoshihisa Murata
Original Assignee
Pfizer Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=47278356&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG11201401032Y(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer Ltd filed Critical Pfizer Ltd
Publication of SG11201401032YA publication Critical patent/SG11201401032YA/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41781,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Rheumatology (AREA)
  • Neurology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
SG11201401032YA 2011-10-26 2012-10-15 (4-phenylimidazol-2-yl) ethylamine derivatives useful as sodium channel modulators SG11201401032YA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161551628P 2011-10-26 2011-10-26
PCT/IB2012/055610 WO2013061205A2 (en) 2011-10-26 2012-10-15 Chemical compounds

Publications (1)

Publication Number Publication Date
SG11201401032YA true SG11201401032YA (en) 2014-07-30

Family

ID=47278356

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201401032YA SG11201401032YA (en) 2011-10-26 2012-10-15 (4-phenylimidazol-2-yl) ethylamine derivatives useful as sodium channel modulators

Country Status (28)

Country Link
US (1) US9079878B2 (en)
EP (1) EP2771335A2 (en)
JP (1) JP5946538B2 (en)
KR (1) KR101586966B1 (en)
CN (1) CN103906746B (en)
AP (1) AP2014007579A0 (en)
AU (1) AU2012328034B2 (en)
BR (1) BR112014009102A2 (en)
CA (1) CA2850925C (en)
CL (1) CL2014000956A1 (en)
CO (1) CO6940427A2 (en)
CR (1) CR20140185A (en)
CU (1) CU20140046A7 (en)
DO (1) DOP2014000085A (en)
EA (1) EA023375B1 (en)
EC (1) ECSP14013324A (en)
GT (1) GT201400079A (en)
HK (1) HK1198650A1 (en)
IL (1) IL232267A (en)
MD (1) MD20140037A2 (en)
MX (1) MX337469B (en)
NI (1) NI201400031A (en)
PE (1) PE20141682A1 (en)
SG (1) SG11201401032YA (en)
TN (1) TN2014000147A1 (en)
UA (1) UA109220C2 (en)
WO (1) WO2013061205A2 (en)
ZA (1) ZA201402281B (en)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103827124B (en) * 2011-09-14 2017-06-06 陶氏益农公司 Method and system for forming boric acid class and its intermediate
GEP20217223B (en) 2013-12-13 2021-02-10 Vertex Pharma Prodrugs of pyridone amides useful as modulators of sodium channels
KR102192572B1 (en) 2014-06-09 2020-12-18 삼성전자주식회사 Method of manufacturing light source module
EP3209303A1 (en) 2014-10-24 2017-08-30 Avectas Limited Delivery across cell plasma membranes
KR20170117170A (en) 2015-02-19 2017-10-20 퍼듀 퍼머 엘피 Methods and compositions for reducing gastric emptying
IS2977B (en) 2015-02-23 2017-07-15 Actavis Group Ptc Ehf. Process for the preparation of intermediates useful in the synthesis of eluxadoline
CN109312315B (en) 2015-12-30 2023-06-09 阿维塔斯有限公司 Carrier-free delivery of gene-editing proteins and compositions to cells and tissues
AU2017292169B2 (en) * 2016-07-06 2021-12-23 Vertex Pharmaceuticals Incorporated Materials and methods for treatment of pain related disorders
JP2019520079A (en) 2016-07-06 2019-07-18 クリスパー セラピューティクス アクチェンゲゼルシャフト Substances and methods for treating pain related disorders
CA3063901A1 (en) 2017-05-16 2018-11-22 Vertex Pharmaceuticals Incorporated Deuterated pyridone amides and prodrugs thereof as modulators of sodium channels
TW201920081A (en) 2017-07-11 2019-06-01 美商維泰克斯製藥公司 Carboxamides as modulators of sodium channels
CN111918650A (en) 2018-02-12 2020-11-10 沃泰克斯药物股份有限公司 Method of treating pain
WO2020146612A1 (en) 2019-01-10 2020-07-16 Vertex Pharmaceuticals Incorporated Esters and carbamates as modulators of sodium channels
US20230062053A1 (en) 2019-01-10 2023-03-02 Vertex Pharmaceuticals Incorporated Carboxamides as modulators of sodium channels
WO2020176763A1 (en) 2019-02-27 2020-09-03 Vertex Pharmaceuticals Incorporated Dosage form comprising prodrug of na 1.8 sodium channel inhibitor
WO2020219867A1 (en) 2019-04-25 2020-10-29 Vertex Pharmaceuticals Incorporated Pyridone amide co-crystal compositions for the treatment of pain
CA3164134A1 (en) 2019-12-06 2021-06-10 Vertex Pharmaceuticals Incorporated Substituted tetrahydrofurans as modulators of sodium channels
EP4347032A1 (en) 2021-06-04 2024-04-10 Vertex Pharmaceuticals Incorporated Substituted tetrahydrofuran-2-carboxamides as modulators of sodium channels
AU2022286511A1 (en) 2021-06-04 2023-11-30 Vertex Pharmaceuticals Incorporated Hydroxy and (halo)alkoxy substituted tetrahydrofurans as modulators of sodium channels
AU2022286438A1 (en) 2021-06-04 2023-11-30 Vertex Pharmaceuticals Incorporated N-(hydroxyalkyl (hetero)aryl) tetrahydrofuran carboxamide analogs as modulators of sodium channels
UY39800A (en) 2021-06-04 2023-01-31 Vertex Pharma N–(HYDROXYALKYL (HETERO)ARYL) TETRAHYDROFURAN CARBOXAMIDES AS SODIUM CHANNEL MODULATORS
AU2022285758A1 (en) 2021-06-04 2023-11-30 Vertex Pharmaceuticals Incorporated Substituted tetrahydrofuran analogs as modulators of sodium channels
KR20240031299A (en) 2021-06-04 2024-03-07 버텍스 파마슈티칼스 인코포레이티드 (2R,3S,4S,5R)-4-[[3-(3,4-difluoro-2-methoxy-phenyl)-4,5-dimethyl-5-(trifluoromethyl)tetrahydrofuran Solid dosage forms and dosing regimens comprising -2-carbonyl]amino]pyridine-2-carboxamide
WO2023205778A1 (en) 2022-04-22 2023-10-26 Vertex Pharmaceuticals Incorporated Heteroaryl compounds for the treatment of pain
US20230373925A1 (en) 2022-04-22 2023-11-23 Vertex Pharma Heteroaryl compounds for the treatment of pain
WO2023205465A1 (en) 2022-04-22 2023-10-26 Vertex Pharmaceuticals Incorporated Heteroaryl compounds for the treatment of pain
WO2023205468A1 (en) 2022-04-22 2023-10-26 Vertex Pharmaceuticals Incorporated Heteroaryl compounds for the treatment of pain
WO2023211990A1 (en) 2022-04-25 2023-11-02 Siteone Therapeutics, Inc. Bicyclic heterocyclic amide inhibitors of na v1.8 for the treatment of pain

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
KR0166088B1 (en) 1990-01-23 1999-01-15 . Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
GB9518953D0 (en) 1995-09-15 1995-11-15 Pfizer Ltd Pharmaceutical formulations
WO2000035298A1 (en) 1996-11-27 2000-06-22 Wm. Wrigley Jr. Company Chewing gum containing medicament active agents
GB9711643D0 (en) 1997-06-05 1997-07-30 Janssen Pharmaceutica Nv Glass thermoplastic systems
US7291641B2 (en) * 1999-10-11 2007-11-06 Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) Derivatives of heterocycles with 5 members, their preparation and their use as medicaments
TWI292316B (en) * 1999-10-11 2008-01-11 Sod Conseils Rech Applic Pharmaceutical composition of thiazole derivatives intended to inhibit mao and/or lipidic peroxidation and/or to act as modulators of sodium channels and the use thereof
US7112366B2 (en) 2001-01-05 2006-09-26 The Ohio State University Chemical monolayer and micro-electronic junctions and devices containing same
TWI248438B (en) * 2001-04-10 2006-02-01 Sod Conseils Rech Applic Derivatives of heterocycles with 5 members, their preparation and their use as medicaments
FR2842808B1 (en) * 2002-07-25 2004-09-10 Sod Conseils Rech Applic NOVEL ARYLIMIDAZOLA DERIVATIVES, THEIR PREPARATION AND THERAPEUTIC APPLICATIONS
US7456164B2 (en) * 2004-05-07 2008-11-25 Pfizer, Inc 3- or 4-monosubtituted phenol and thiophenol derivatives useful as H3 ligands
PT1747210E (en) * 2004-05-07 2010-08-31 Warner Lambert Co 3- or 4-monosubstituted phenol and thiophenol derivatives useful as h3 ligands
US7786291B2 (en) 2004-10-27 2010-08-31 Schering Corporation Compositions and methods for short interfering nucleic acid inhibition of Nav1.8
RS54522B1 (en) 2005-12-22 2016-06-30 Newron Pharmaceuticals S.P.A. 2-phenylethylamino derivatives as calcium and/or sodium channel modulators
AP2780A (en) 2006-10-18 2013-09-30 Pfizer Prod Inc Biaryl ether urea compounds
EP1995241B1 (en) 2007-03-23 2010-03-17 ICAgen, Inc. Inhibitors of ion channels
JP2010526051A (en) * 2007-05-03 2010-07-29 ファイザー・リミテッド N- [6-amino-5- (phenyl) pyrazin-2-yl] -isoxazole-4-carboxamide derivatives and related compounds as NAV1.8 channel modulators for the treatment of pain
MX2009011816A (en) 2007-05-03 2009-11-19 Pfizer Ltd 2 -pyridine carboxamide derivatives as sodium channel modulators.
CA2693588C (en) 2007-07-13 2015-11-17 Icagen, Inc. Sodium channel inhibitors

Also Published As

Publication number Publication date
TN2014000147A1 (en) 2015-09-30
BR112014009102A2 (en) 2017-04-18
CA2850925A1 (en) 2013-05-02
US20140296313A1 (en) 2014-10-02
CL2014000956A1 (en) 2014-07-18
HK1198650A1 (en) 2015-05-22
WO2013061205A3 (en) 2013-06-27
WO2013061205A2 (en) 2013-05-02
ZA201402281B (en) 2015-11-25
CU20140046A7 (en) 2014-10-02
EA201490864A1 (en) 2014-08-29
IL232267A (en) 2016-10-31
CR20140185A (en) 2014-06-03
CO6940427A2 (en) 2014-05-09
CN103906746B (en) 2015-12-09
EA023375B1 (en) 2016-05-31
MX2014004738A (en) 2014-08-01
JP5946538B2 (en) 2016-07-06
WO2013061205A8 (en) 2014-03-27
CN103906746A (en) 2014-07-02
MD20140037A2 (en) 2014-08-31
CA2850925C (en) 2017-01-10
KR20140069234A (en) 2014-06-09
PE20141682A1 (en) 2014-11-14
UA109220C2 (en) 2015-07-27
AP2014007579A0 (en) 2014-04-30
ECSP14013324A (en) 2014-05-31
JP2014530900A (en) 2014-11-20
US9079878B2 (en) 2015-07-14
IL232267A0 (en) 2014-06-30
AU2012328034B2 (en) 2015-04-23
MX337469B (en) 2016-03-02
KR101586966B1 (en) 2016-01-19
GT201400079A (en) 2015-06-02
NZ623090A (en) 2015-10-30
NI201400031A (en) 2014-10-01
DOP2014000085A (en) 2014-08-31
AU2012328034A1 (en) 2014-05-15
EP2771335A2 (en) 2014-09-03

Similar Documents

Publication Publication Date Title
HK1198650A1 (en) (4-phenylimidazol-2-yl) ethylamine derivatives useful as sodium channel modulators (4--2-)
HK1238627A1 (en) Fused heterocyclic compounds as sodium channel modulators
HK1200713A1 (en) Benzyl sulfonamide derivatives as rorc modulators rorc
SI2581991T1 (en) Holder frame for connector
HK1201526A1 (en) Benzyl sulfonamide derivatives as rorc modulators rorc
PT2663550T (en) Substituted benzoazepines as toll-like receptor modulators
EP2663555A4 (en) Substituted benzoazepines as toll-like receptor modulators
EP2794880A4 (en) Methods for modulating metastasis-associated-in-lung-adenocarcinoma-transcript-1(malat-1) expression
EP2709985A4 (en) Amine derivatives as potassium channel blockers
EP2568021B8 (en) Ink Composition
EP2661179A4 (en) Reduced sodium composition
EP2676553A4 (en) Carotenoid-containing composition
HK1190884A1 (en) Carotenoid coloring composition
EP2659313A4 (en) Printing
HK1179956A1 (en) Fused heterocycic derivatives as s1p modulators s1p
IL233001A0 (en) Novel iso-ergoline derivatives
EP2688426A4 (en) Reduced sodium salt composition
HK1196605A1 (en) 2-oxo-piperidinyl derivatives 2--
AU2012902375A0 (en) Low sodium salt
AU2011903092A0 (en) Improvements Relating To Printing
GB201106990D0 (en) Connector for frames
GB201101084D0 (en) Connector for frames
GB201220680D0 (en) Antibacterials
AU2011903834A0 (en) Alignment Apparatus
AU2011903178A0 (en) 888-SuperPower (KineticEnergy2ElectricPower)